Identification of rare copy number variations reveals PJA2, APCS, SYNPO, and TAC1 as novel candidate genes in Autism Spectrum Disorders

BACKGROUND: There is a strong evidence for genetic factors as the main causes of Autism Spectrum Disorders (ASD). To date, hundreds of genes have been identified either by copy number variations (CNVs) and/or single nucleotide variations. However, despite all the findings, the genetics of these diso...

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Detalhes bibliográficos
Publicado no:Mol Genet Genomic Med
Main Authors: Bitar, Tania, Hleihel, Walid, Marouillat, Sylviane, Vonwill, Sandrine, Vuillaume, Marie‐Laure, Soufia, Michel, Vourc'h, Patrick, Laumonnier, Frederic, Andres, Christian R.
Formato: Artigo
Idioma:Inglês
Publicado em: John Wiley and Sons Inc. 2019
Assuntos:
Original Articles
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6687626/
https://ncbi.nlm.nih.gov/pubmed/31254375
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/mgg3.786
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